Methanol → HCID 86742519, compound

HRID 2231401Notes

Reaction equation

HRID 2231401 reaction equation
C(OC=CC[S:8]C)(=O)C.CO.[C]=O.[C:14]([O:17][CH:18]([CH2:23][CH2:24][S:25][CH3:26])[C:19]([O:21][CH3:22])=O)(=[O:16])[CH3:15]>C1C=CC=CC=1.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1(C)C=CC=CC=1>[C:14]([O:17][CH:18]([CH2:23][CH2:24][S:25][CH3:26])[C:19]([O:21][CH3:22])=[S:8])(=[O:16])[CH3:15]

Participants

8

Conditions

Temperature
100 °C

Procedure

0.5 mmoles 1-acetoxy-3-methylthiopropene, (Z:E ratio 43:57) and 2.5 mmoles methanol were charged into a 71 cc stainless steel. bomb equipped with a glass liner and a Teflon coated stir bar. Ten mole percent, based on 1-acetoxy-3methythiopropene, of a catalyst comprising bis(triphenylphosphine)dichloropalladium, (φ3P)2PdCl2, was added. Toluene was included as an internal standard. Five milliliters of benzene as a solvent were also included in the reaction system. The reaction mixture was charged under argon. The bomb was sealed and carbon monoxide at a pressure of 1000 psi (at room temperature) was charged to the bomb, and the bomb was heated to 100° C. and allowed to react for 44 hours with stirring. At the termination of the reaction, the reaction products were analyzed by gas chromatography and it was found that 2-acetoxy-4-(methylthio)butanoic acid, methyl ester was produced in a yield of 22 percent, and that 2-acetoxy-4-(methylthio)thiobutanoic acid, methyl ester was produced in a yield of 10 percent, based on the 1-acetoxy-3-methylthiopropene reactant charged. Each of the products is hydrolyzable to methionine hydroxy analog.

Workup

  1. custombomb equipped with a glass liner and a Teflon coated stir bar
  2. additionwas added
  3. additionThe reaction mixture was charged under argon
  4. customThe bomb was sealed
  5. customto react for 44 hours
  6. customAt the termination of the reaction
  7. customwas produced in a yield of 22 percent

Sources & evidence

ORD record
ord-82b8f1b1a9b84e6eb307d769a42e5c58
Source dataset
uspto-grants-1988_11
Patent number
US04782173

Reaction notes

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